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Protein encapsulation in and release from monodisperse double-wall polymer microspheres

机译:蛋白质包裹在单分散双壁聚合物微球中或从中释放

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摘要

Biodegradable polymer double-wall microspheres (DWMS) are promising vehicles for macromolecular therapeutics such as proteins and peptides. Using precision particle fabrication (PPF) technology, uniform DWMS with outer diameter ~55 μm were fabricated comprising poly(lactide-co-glycolide) cores encapsulating bovine serum albumin (BSA) and ~10 μm thick, drug-free, poly(lactic acid) shells of varying PLA molecular weight. Also, monolithic single-wall microspheres (SWMS) were fabricated to mimic the BSA-loaded core. The use of relatively fast extracting ethyl acetate and slowly extracting dichloromethane as shell- and core-phase solvents, respectively, was found to produce DWMS with well-defined core-shell structure, high BSA encapsulation efficiency, and the desired localization of protein in the particle core. Initial protein distribution, particle erosion, and in vitro protein release from DWMS and SWMS were examined. The presence of a BSA-free shell in DWMS decreased the protein release rate and extended the duration of release from ~50 days to 70-80 days, demonstrating the capacity of such DWMS to provide enhanced control of protein delivery rates.
机译:可生物降解的聚合物双壁微球(DWMS)是用于蛋白质和肽等大分子治疗剂的有前途的载体。使用精密颗粒制造(PPF)技术,制造了外径约为55μm的均匀DWMS,包括包裹牛血清白蛋白(BSA)和约10μm厚,无药物的聚乳酸的聚(丙交酯-共-乙交酯)核)不同PLA分子量的炮弹。此外,还制作了整体式单壁微球(SWMS)来模拟加载BSA的核心。发现分别使用相对快速的乙酸乙酯和缓慢萃取的二氯甲烷作为壳层和核心相溶剂,可生产出具有明确定义的核-壳结构,高BSA包封效率和所需蛋白质在蛋白质中定位的DWMS。粒子核。检查了最初的蛋白质分布,颗粒侵蚀以及DWMS和SWMS的体外蛋白质释放。 DWMS中无BSA外壳的存在降低了蛋白质释放速率,并将释放持续时间从约50天延长至70-80天,证明了此类DWMS提供增强的蛋白质释放速率控制能力。

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